CN100344447C - Thin film lamination-delamination process for fluoropolymers - Google Patents

Thin film lamination-delamination process for fluoropolymers Download PDF

Info

Publication number
CN100344447C
CN100344447C CNB2004800081893A CN200480008189A CN100344447C CN 100344447 C CN100344447 C CN 100344447C CN B2004800081893 A CNB2004800081893 A CN B2004800081893A CN 200480008189 A CN200480008189 A CN 200480008189A CN 100344447 C CN100344447 C CN 100344447C
Authority
CN
China
Prior art keywords
carrier layer
layer
receiver sheet
ethylene
copolymer
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
CNB2004800081893A
Other languages
Chinese (zh)
Other versions
CN1764538A (en
Inventor
M·J·彻尔平斯基
Y·P·R·婷
J·D·穆尔顿
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Honeywell International Inc
Original Assignee
Honeywell International Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Honeywell International Inc filed Critical Honeywell International Inc
Publication of CN1764538A publication Critical patent/CN1764538A/en
Application granted granted Critical
Publication of CN100344447C publication Critical patent/CN100344447C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
    • B32B27/304—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising vinyl halide (co)polymers, e.g. PVC, PVDC, PVF, PVDF
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
    • B32B27/322—Layered products comprising a layer of synthetic resin comprising polyolefins comprising halogenated polyolefins, e.g. PTFE
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B38/00—Ancillary operations in connection with laminating processes
    • B32B38/18—Handling of layers or the laminate
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B43/00—Operations specially adapted for layered products and not otherwise provided for, e.g. repairing; Apparatus therefor
    • B32B43/006—Delaminating
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
    • B32B7/02—Physical, chemical or physicochemical properties
    • B32B7/027—Thermal properties
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
    • B32B7/04—Interconnection of layers
    • B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00—Properties of the layers or laminate
    • B32B2307/30—Properties of the layers or laminate having particular thermal properties
    • B32B2307/308—Heat stability
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2327/00—Polyvinylhalogenides
    • B32B2327/12—Polyvinylhalogenides containing fluorine
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2553/00—Packaging equipment or accessories not otherwise provided for
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B37/00—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding
    • B32B37/02—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by a sequence of laminating steps, e.g. by adding new layers at consecutive laminating stations
    • B32B37/025—Transfer laminating
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B37/00—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding
    • B32B37/12—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by using adhesives
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B37/00—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding
    • B32B37/14—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers
    • B32B37/15—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers with at least one layer being manufactured and immediately laminated before reaching its stable state, e.g. in which a layer is extruded and laminated while in semi-molten state
    • B32B37/153—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers with at least one layer being manufactured and immediately laminated before reaching its stable state, e.g. in which a layer is extruded and laminated while in semi-molten state at least one layer is extruded and immediately laminated while in semi-molten state
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
    • Y10T428/24942—Structurally defined web or sheet [e.g., overall dimension, etc.] including components having same physical characteristic in differing degree
    • Y10T428/2495—Thickness [relative or absolute]
    • Y10T428/24959—Thickness [relative or absolute] of adhesive layers
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
    • Y10T428/24942—Structurally defined web or sheet [e.g., overall dimension, etc.] including components having same physical characteristic in differing degree
    • Y10T428/2495—Thickness [relative or absolute]
    • Y10T428/24967—Absolute thicknesses specified
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]

Landscapes

  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Laminated Bodies (AREA)
  • Moulding By Coating Moulds (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

A process for forming thin film laminations of thin fluoropolymer films to receiver sheets, more particularly, the production of very thin, transferable fluoropolymer films. A thin fluoropolymer base layer is applied onto a support layer, which may be a thicker film. The support layer/thin base layer is then laminated to a receiver sheet, followed by stripping away the support layer, leaving the base film on the receiver sheet.

Description

The thin film lamination-delamination process that is used for fluoropolymer
Background of invention
Invention field
The present invention relates to the film lamination of fluoro-containing copolymer film and polymer receiver sheet.More particularly, the present invention relates to produce extremely thin, transferable various fluoro-containing copolymer films with improvement heat endurance.
Association area is described
Be well known in the art and produce individual layer and multilayer fluorine-contained thin polymer film.For example referring to United States Patent (USP) 4,677,017,4,659,625 and 5,139,878.Because fabulous protection against the tide and vapor barrier properties, it is known that many fluorinated polymer materials are generally people, is the required component of packaging film therefore, is used in particular for lid (lidding) film and blister package.Also need to be orientated the characteristic of this film in some applications with further this film of raising.For example, do the lid worn, can push the lane and wear and obtain product, need this film of uniaxial orientation in order to obtain a direction for the pushing that is used for medicine packing.For high-intensity lid film, need biaxially oriented film.Compare with non-oriented fluoropolymers film, the fluoro-containing copolymer film of orientation also shows improved moisture barrier properties comprises.
Because the difficult especially orientation of the crystalline rate and the thermal induction auto-orientation that are exceedingly fast, fluoropolymer (for example polytrifluorochloroethylene (PCTFE)).The structure of the highly crystalline that the fast crystallization rate of PCTFE produces has hindered orientation, is actually after to a certain degree to have hindered further orientation.Its thermal induction auto-orientation causes this film not extend certainly at machine traffic direction or longitudinal stretching direction when having the constraint heating, and cross-direction shrinkage.United States Patent (USP) 4,510,301 disclose the oriented film that contains 40-60% molar ethylene and chlorotrifluoroethylene.United States Patent (USP) 4,519,969 disclose biaxially oriented film and the manufacture method thereof that contains at least 90% molar ethylene-TFE copolymer.Also the multilayer fluorine-contained structured polymer film that production is contained the fluoropolymer thin layer has carried out various effort.Emphasis concentrates on the selection jointing material mostly.United States Patent (USP) 4,677,017 discloses by using the co-extrusion plural layers that comprise fluoropolymer and thermoplastic film of binder polymer adhesion.United States Patent (USP) 4,659,625 disclose the fluoropolymer multi-layer film structure that uses the vinyl acetate polymer adhesive layer.Be attached to the United States Patent (USP) 5,139,878 that comes by reference herein and disclose the fluoropolymer film structure of using the adhesive layer of improved polyalkene.But, need a kind of fluoro-containing copolymer film that is applicable to multilayered packaging film in this area.
Also need to use conventional equipment in this area, produce stretchable and transferable fluoro-containing copolymer film at low cost.Existing fluoro-containing copolymer film laminated material has been subjected to the laminating method relevant with handling extremely thin film and the restriction of cost, therefore need form thick fluoro-containing copolymer film on receiver sheet.Specifically, because the restriction of extrusion method and laminating method, existing known technology needs the minimum thickness of fluoro-containing copolymer film to be at least about 50 units (gauge) (0.5 mil, 12.5 μ m).Particularly, because coextrusion coating or extrude applying method and need high melting temperature, make that can not accept material (for example polyvinyl chloride (PVC)) at some polymer goes up and introduce fluoro-containing copolymer film.Therefore, for lamination on PVC, coextrusion coating or extrude some fluoro-containing copolymer film of fitting, need to use thicker fluoro-containing copolymer film.But, in some applications, need thin fluoro-containing copolymer film, promptly the thickness of fluoro-containing copolymer film is about 4 units (0.04 mil, 1 μ m)-Yue 40 units (0.4 mil, 10.2 μ m).
As mentioned above, the fluoro-containing copolymer film of known orientation shows improved performance, but existing processing limitation has also limited the degree of orientation that carries out on the carrier-free fluoro-containing copolymer film.Therefore, need to have good humidity resistance and thickness fluoro-containing copolymer film laminated material in this area less than about 40 units (0.4 mil, 10.2 μ m).
Summary of the invention
The invention provides a kind of thin film lamination-delamination process, said method comprising the steps of:
A) provide carrier layer with first and second surfaces;
B) the thin base fluoropolymer layer of one deck at least that will have first and second surfaces is applied at least one surface of described carrier layer, and the first surface of the described bottom of one deck at least contacts with the surface of described carrier layer;
C) adhesive layer is applied to the described second surface of described bottom;
D) make described bottom be attached to receiver sheet by described adhesive layer; With
E) separate described carrier layer from described bottom, make described bottom still be attached to described receiver sheet.
The present invention also provides a kind of plural layers, and described plural layers comprise:
A) has the carrier layer on first and second surfaces;
B) at least one lip-deep thin base fluoropolymer layer of one deck at least with first and second surfaces of described carrier layer, the first surface of the described bottom of one deck at least contacts with the surface of described carrier layer; The thickness of wherein said bottom is less than or equal to about 0.4 mil (10.2 μ m);
C) adhesive layer on the second surface of described bottom; With
D) be attached to the receiver sheet of described bottom, make described adhesive layer contact with described receiver sheet.
The present invention also provides a kind of plural layers, and described plural layers comprise:
A) has surperficial receiver sheet; With
B) be attached to the thin base fluoropolymer layer of described receiver sheet;
The thickness of wherein said bottom is for being less than or equal to about 0.4 mil (10.2 μ m), and wherein said thin bottom is attached to receiver sheet by intermediate adhesion layer through lamination.
The invention provides the method for a kind of thin base fluoropolymer layer and carrier layer coextrusion, wherein coextrusion shows that the plunger bond strength between fluoropolymer layer and the carrier layer is low.Be at least 50 units (about 12.5 μ m) with the thickness of the existing known method needs in this area and compare, the thickness of base fluoropolymer layer of the present invention is preferably about 4 units (about 1 μ m)-Yue 40 units (about 10.2 μ m).Carrier layer can be thicker film, and thickness is more than or equal to about 1 mil (about 25 μ m).Plunger bond strength is enough to make co-extruded films and receiver sheet adhesive lamination, and not delamination and mechanical delamination subsequently on the carrier layer, the base fluoropolymer layer that one deck is extremely thin has been stayed on the receiver sheet.
Detailed description of the preferred embodiments
The invention provides thin film lamination-delamination process, wherein the coextrusion layer of the thin base fluoropolymer layer of self-supporting (self-supporting) and polymer carrier layer is by intermediate adhesion layer and receiver sheet lamination, with the carrier layer delamination, will approach base fluoropolymer layer and stay on the receiver sheet subsequently.Described carrier layer has first and second surfaces, has formed the thin base fluoropolymer layer with first and second surfaces with the fluorinated polymer material coextrusion, and the first surface of described bottom is on the second surface of described carrier layer.Subsequently adhesive layer is applied to the second surface of described bottom.With this structure and receiver sheet lamination, make adhesive layer contact subsequently with the surface of receiver sheet.After the lamination step, separate receiver sheet and carrier layer, bottom and adhesive layer are stayed on the receiver sheet.
The well-known fluoropolymer material has excellent chemical resistance, release property and protection against the tide and vapor barrier properties, is the required component of packaging film therefore.It should be understood that this thin bottom is the self-supporting film, can entirely be transferred to another ground from a ground.In embodiment preferred of the present invention, this thin fluoropolymer layer can be made up of fluoropolymer homopolymers or its copolymer or blend, these fluoropolymers as well known in the art, and at for example United States Patent (USP) 4,510,301,4,544,721 and 5,139, described in 878.Preferred fluoropolymer includes but not limited to ethylene-chlorotrifluoro-ethylene copolymer, ethylene-tetrafluoroethylene copolymer, fluorinated ethylene-propylene copolymer, perfluoroalkyl ethylene oxy, polytrifluorochloroethylene, polytetrafluoroethylene (PTFE), polyvinyl fluoride, polyvinylidene fluoride and copolymer thereof and blend.Most preferred fluoropolymer comprises the homopolymers and the copolymer of polytrifluorochloroethylene.Particularly preferred is PCTFE material (trade mark is ACLAR , and Honeywell InternationalInc. (Morristown, New Jersey) sells).
When preparation plural layers of the present invention, thin base fluoropolymer layer and carrier layer coextrusion.Bottom and carrier layer all have first and second surfaces and adhered to one another, make the first surface of bottom contact with the second surface of carrier layer.The suitable carriers layer material comprises and is selected from following material: polyamide, polyolefin, polyvinyl chloride (PVC), polyurethane, ethylene-vinyl acetate (EVA), polyester (for example PET (PET)), cyclic olefin polymer (homopolymers and copolymer) and above-mentioned one or more blend.
Here the polyolefin that is fit to use comprises the polymer of the 'alpha '-olefin monomers with about 6 carbon atoms of about 2-, comprises homopolymers, copolymer (comprising graft copolymer) and the terpolymer of alpha-olefin.The example of exemplary homopolymers comprises ultra-low density polyethylene (ULDPE), low density polyethylene (LDPE) (LDPE), linear low density polyethylene (LLDPE) (LLDPE), metallocene linear low density polyethylene (LLDPE) (m-LLDPE), medium density polyethylene (MDPE), high density polyethylene (HDPE) (HDPE), polypropylene, polybutene, poly-1-butylene, poly 3 methyl butene 1, poly-1-amylene, poly(4-methyl-1-pentene), polyisobutene, polyhexene and combination thereof.
Polyolefin (for example various polyethylene) is distinguished based on density usually, is distinguished by the density that the number of per 1,000 contained side chain of carbon atom obtains on the polyethylene main chain in the molecular structure.Side chain is generally C 3-C 8Alkene is preferably butylene, hexene or octene.For example, HDPE short-chain branch number (per 1,000 carbon atom is less than 20) is considerably less, has caused higher density (being that density range is about 0.94 gram/cubic centimetre-Yue 0.97 gram/cubic centimetre).LLDPE has more short-chain branch number (per 1,000 carbon atom is 20-60), and density is the about 0.93 gram/cubic centimetre of about 0.91-.The density of LDPE is the about 0.93 gram/cubic centimetre of about 0.91-, contains long-chain branch (per 1,000 carbon atom be 20-40), rather than contained among LLDPE and the HDPE be short-chain branch.ULDPE is than the short-chain branch density of LLDPE and HDPE higher (being that per 1,000 carbon atom is about 250 of about 80-), and density is the about 0.91 gram/cubic centimetre of about 0.88-.Exemplary copolymer and ter-polymers comprise the copolymer and the ter-polymers of alpha-olefin and other alkene, for example ethylene-propylene copolymer, ethylene-butene copolymer, ethene-pentene copolymer, ethene-hexene copolymer and ethylene-propylene-diene copolymer (EPDM).Term polyolefin used herein also comprise acrylonitrile-butadiene-styrene (ABS) (ABS) polymer and with the copolymer of vinylacetate, acrylate and methacrylate etc.Preferred polyolefin is those polyolefin by the alpha-olefin preparation, the most preferably polymer of ethene, copolymer and ter-polymers.Above polyolefin can be made by any known method.It is about 1 that polyolefinic mean molecule quantity can be, and 000-is about 1,000,000, is preferably approximately 10, and 000-about 500,000.Preferred polyolefin is polyethylene, polypropylene, polybutene and copolymer thereof and blend.Most preferred polyolefin is a polyethylene.Most preferred polyolefin is a low density polyethylene (LDPE).
Suitable polyamide (nylon) within the scope of the present invention not only (non-exclusively) comprises that molecular weight is about 10, homopolymers that is selected from aliphatic polyamide and aliphatic/aromatic polyamides or the copolymer of 000-about 100,000.The conventional method that is used to prepare polyamide is that this area is well-known, comprises the reaction from condensation and diacid and diamines of lactams.
Available polyamide homopolymer comprises poly-4-aminobutyric acid (nylon 4), poly-6-aminocaprolc acid (nylon 6, also be called polycaprolactam), poly-7-aminoheptylic acid (nylon 7), poly(8 amino caprylic acid) (nylon 8), poly-9 aminononanoic acid (nylon 9), the amino capric acid (nylon 10) of poly-10-, the amino hendecanoic acid (nylon 11) of poly-11-, poly-12 amino dodecanoic acid (nylon 12), nylon 4,6, polyhexamethylene adipamide (nylon 6,6), polyhexamethylene sebacamide (nylon 6,10), poly-heptanedioyl heptamethylene diamine (nylon 7,7), poly-suberoyl octamethylenediamine (nylon 8,8), poly-nonanedioyl hexamethylene diamine (nylon 6,9), poly-nonanedioyl nonamethylene diamine (nylon 9,9), poly-nonanedioyl decamethylene diamine (nylon 10,9), 1,4-butanediamine-oxalic acid copolymer (nylon 4,2), the polyamide of n-dodecane diacid and hexamethylene diamine (nylon 6,12), the polyamide of dodecane diamines and n-dodecane diacid (nylon 12,12) etc.Available aliphatic polyamide copolymers comprises caprolactam/hexamethylene adipamide copolymer (nylon 6,6/6), hexamethylene adipamide/caprolactam copolymer (nylon 6/6,6), adipyl propane diamine/nonanedioyl hexamethylene diamine copolymer (nylon trimethyl 6,2/6,2), hexamethylene adipamide-nonanedioyl hexamethylene diamine-caprolactam copolymer (nylon 6,6/6,9/6) etc.Also comprise not special other various nylon of describing here.In these polyamide, preferred polyamide comprises nylon 6, nylon 6,6, nylon 6/6,6, nylon 6,6/6 and composition thereof.Most preferred nylon is nylon 6.
Can be applied to aliphatic polyamide of the present invention can prepare by commercial source or according to known technology.For example polycaprolactam can derive from Honeywell International Inc., Morristown, and New Jersey, trade mark are CAPRON .
The example of aliphatic/aromatic polyamides comprise poly-between phenyl-diformyl butanediamine (nylon 4, I), poly-6I hexamethylene isoterephalamide (nylon 6, I), hexamethylene adipamide/6I hexamethylene isoterephalamide copolymer (nylon 6,6/6I), hexamethylene adipamide/hexamethylene terephthalamide copolymer (nylon 6,6/6T), poly-paraphenylene terephthalamide 2,2,2-trimethyl hexamethylene diamine, poly hexamethylene adipamide m-xylylene amine (MXD6), poly hexamethylene adipamide is to xylylene amine, poly-hexamethylene terephthalamide, poly-paraphenylene terephthalamide's dodecane diamines, polyamide 6 T/6I, polyamide 6/MXDT/I, polyamide MXDI etc.Also can use the blend of two or more aliphatic/aromatic polyamides.Aliphatic/aromatic polyamides can be prepared by known technology of preparing or be obtained by commercial source.At United States Patent (USP) 4,826, other suitable polyamide have been described in 955 and 5,541,267, this patent is attached to herein by reference.
For example at United States Patent (USP) 5,218, suitable cyclic olefin polymer (homopolymers, copolymer or blend) has been described in 049,5,783,273 and 5,912,070, this patent is attached to herein by reference.United States Patent (USP) 5,218,049 discloses the various films of being made up of cycloolefin.United States Patent (USP) 5,783,273 disclose the pressure that comprises the cyclic olefine copolymer sheet material wears the blister package material.United States Patent (USP) 5,912,070 discloses the packaging material that comprise one deck cycloolefin, one deck polyester and intermediate adhesion layer.In the middle of these materials, the copolymer of optimal ethylene and ENB.
In an embodiment preferred of the present invention, carrier layer and base fluoropolymer layer can be chosen wantonly and the intermediate adhesion layer coextrusion between carrier layer and bottom.This optional adhesive layer can comprise anhydride modified alpha-olefin, polypropylene, hexenoic acid (ethlene acid) copolymer resin, acrylic or methacrylic acid modified copolymer, metallocene polymerising ethylene copolymer (ethene/cyclic olefine copolymer for example, ethylene/styrene, ethene/long side chain (long side chains)), ethylene-vinyl acetate copolymer, sour and anhydride modified polyacrylate and olefin-acrylic ester copolymer, epoxide modified polyolefin, sour and anhydride modified elastomer, s-B-S (SBS) rubber and blend thereof.
After base fluoropolymer layer and carrier layer combine, adhesive layer is coated on the second surface of bottom.Can use any suitable jointing material, comprise those above-mentioned jointing materials.Other suitable adhesive polymers comprise polyurethane, epoxides, polyester, acrylic compounds, modified polyolefin compositions, and these polymer have at least one functional moiety who is selected from unsaturated polybasic carboxylic acid and acid anhydrides thereof.Same suitable adhesive polymer is the blend of these materials.This class unsaturated carboxylic acid and acid anhydrides comprise maleic acid and maleic anhydride, fumaric acid and fumaric acid anhydride, crotonic acid and crotonic anhydride, citraconic acid and citraconic anhydride, itaconic acid and itaconic anhydride etc.Be suitable for improved polyalkene of the present invention and comprise United States Patent (USP) 3,481, the composition of describing in 910,3,480,580,4,612,155 and 4,751,270.Other adhesive layers not only comprise as United States Patent (USP) 5,139, alkene described in 878 and α, the alkyl ester copolymer of the Arrcostab of β-ethylenically unsaturated carboxylic acids.Preferred modified polyolefin compositions is included as the functional moiety of about 0.001-about 20% of improved polyalkene gross weight.More preferably functional moiety's amount is about 10% weight of about 0.05-, most preferably is about 5% weight of about 0.1-.As United States Patent (USP) 5,139,878 descriptions, modified polyolefin compositions also can comprise thermoplastic elastomer (TPE) and the Arrcostab that reaches as high as about 40% weight.Preferred polyurethane binder comprises two-component polyurethane systems (solvent base and water base) or single-component system.Preferred epoxy adhesive is the bi-component epoxy adhesive composition that is formed by epoxides and amine reaction.Preferred acrylic adhesives comprises contact adhesive.Same suitable bonding is 100% solid binder through ultraviolet or electronic beam curing.Can come applied adhesives by any suitable method in this area (for example coating or co-extrusion).Any of these jointing material can be used as the intermediate adhesion layer between carrier layer and base fluoropolymer layer, and this is also in the preferred embodiments of the invention scope.
In case adhesive layer is applied to bottom, preferably support/base/adhesive structure is attached to receiver sheet by following lamination.Suitable receiver sheet comprises and is selected from following material: polyolefin, polyvinyl chloride, polyester, polyamide, ethylene-propylene acetoacetic ester, ethylene-acrylic acid or cyclic olefin polymer.Suitable polyolefin comprises above-mentioned polyolefin.As known in the art, can carry out metalized to these layers.Receiver sheet also can comprise any other suitable polymers film, fabric (woven or non-woven) or paper ground.Receiver sheet is preferably plastic material, and more preferably PVC, polyolefin or cycloolefin are preferably formed by extrusion.In order to improve bonding with bottom, before lamination step, can choose wantonly receiver sheet through sided corona treatment, this is also within the scope of the invention.Sided corona treatment is a kind of like this method, and by corona discharge assembly, the surface that makes this layer is with going up electric charge to improve the adhesive capacity of itself and adjacent layer with one deck of material.If carry out corona discharge, preferably after forming, receiver sheet carries out immediately.
Behind support/base/adhesive structure and the receiver sheet lamination, use technology well-known in the art, with receiver sheet carrier is separated from bottom by delamination or by tearing carrier layer.The delamination step will approach base fluoropolymer layer and stay on the receiver sheet.Therefore, can be retained on the receiver sheet, must make bonding strength between bottom and the receiver sheet be greater than plunger bond strength between bottom and the carrier layer in order to make bottom.Bonding strength between preferred bottom and the receiver sheet is at least about 2 times of plunger bond strength between bottom and the carrier layer, more preferably is at least about 3 times.In a preferred embodiment, plunger bond strength between bottom and the carrier layer is less than about 90g/ inch (35g/cm), and the plunger bond strength between bottom and the receiver sheet is preferably greater than about 200g/ inch (79g/cm), more preferably greater than about 300g/ inch (118g/cm).Therefore, when tearing receiver sheet and carrier layer, destroyed bonding between bottom and the carrier layer, bottom has been stayed on the receiver sheet.
Carrier layer, base fluoropolymer layer, adhesive layer and receiver sheet also all can be chosen wantonly and comprise one or more conventional additives, and using to those skilled in the art of these additives is well-known.In the processing that will improve composition and when improving, can need to use examples of such additives by its product that forms or goods.The example of this class additive comprises oxidation and heat stabilizer, lubricant, releasing agent, fire retardant, oxidation retarder, oxidation scavengers, dyestuff, pigment and other colouring agents, UV absorbers and stabilizing agent, organic or inorganic filler (comprising particulate filler and fiberfill), reinforcing agent, nucleator, plasticizer and other conventional additives well known in the art.With respect to whole composition layer, the consumption of examples of such additives for example reaches as high as about 10% weight.
Plural layers of the present invention can be produced by the conventional method that is used to produce plural layers (comprising co-extrusion and lamination).In embodiment preferred of the present invention, carrier layer and base fluoropolymer layer preferably adhere to by co-extrusion.For example, the macromolecular material that is respectively applied for each layer is added in horizontal feed (infeed) feed hopper of extruder of similar number, each extruder is handled one or more layers material.Will be in the fusion and the co-extrusion mouth mould that flows to a manifold of plasticating of each extruder.In this mouthful mould, each layer is juxtaposed and combined, discharge from the mouth mould as one deck plural layers of macromolecular material subsequently.After coming out from the mouth mould, this film rolls on the first temperature control stretcher roll, through first roller, goes up calendering at the second temperature control roller (lower than first roller temperature usually) subsequently.These controlled temperature rolls have been controlled the cooldown rate after film comes out to a great extent from the mouth mould.Also can use other rollers.In another approach, film-forming apparatus can be the equipment that is known as inflation film equipment in the art, comprise the cylindrical mouthful mould of the manifold (multi-manifold) that is used for the bubbling blown film, the film composition after the plasticizing is stressed by this mouthful mould and form the film bubble, squeezes flat at last and forms film.The method of co-extrusion film forming and receiver sheet lamination is generally known.At United States Patent (USP) 5,139, typical co-extrusion technology has been described in 878 and 4,677,017.
An advantage of co-extrusion film is that one-step method has formed plural layers, and the melting layer combination by with each thin layer of carrier layer, base fluoropolymer layer and any other optional thin layer has formed whole membrane structure.
Art methods need be with thick fluoro-containing copolymer film (thickness is about 12.5 μ m greater than 0.5 mil) and suitable receiver sheet lamination so far.Lamination of the present invention-delamination method can allow thin film (thickness is about 0.04 mil (about 1 μ m)-Yue 0.4 mil (about 10.2 μ m)) be applied on this type of above-mentioned required receiver sheet.
Can be before adhering to receiver sheet, will with the combination orientation of the base fluoropolymer layer of carrier layer adhesion.For the present invention, the term draw ratio is meant the increase in the draw direction size.The stretchable draw ratio of this layer is 1.5: 1-5: 1, and for the uniaxial tension (promptly vertical or horizontal) of at least one direction or the vertical and horizontal both direction is biaxial stretch-formed.This layer is biaxial orientation simultaneously, for example laterally film is orientated simultaneously at machine direct of travel and its.This has caused at the transparency, intensity and toughness aspect of performance surprising improvement being arranged, and has improved moisture vapor transmission rate simultaneously.
Though each of multi-layer film structure layer has different thickness, the preferred thickness of carrier layer is about 1 mil (25 μ m)-Yue 6 mils (150 μ m), more preferably about 2 mils (50 μ m)-Yue 5 mils (125 μ m) most preferably are about 3 mils (75 μ m)-Yue 4 mils (100 μ m).The thickness of thin bottom is about 0.04 mil (1 μ m)-Yue 0.4 mil (10.2 μ m), and preferred thickness is about 0.08 mil (2 μ m)-Yue 0.4 mil (10.2 μ m), more preferably about 0.21 mil (5 μ m)-Yue 0.31 mil (8 μ m).The preferred thickness of adhesive layer is about 0.04 mil (1 μ m)-Yue 0.4 mil (10.2 μ m), more preferably about 0.12 mil (3 μ m)-Yue 0.31 mil (8 μ m).The preferred thickness of receiver sheet is about 0.2 mil (5 μ m)-Yue 12 mils (300 μ m), and more preferably about 0.4 mil (10.2 μ m)-Yue 8 mils (200 μ m) most preferably is about 0.6 mil (15 μ m)-Yue 4 mils (100 μ m).Though can it should be understood that other bed thickness is wanted to satisfy special demand, then still within the scope of the invention with reference to these thickness.
Plural layers of the present invention can be used as planar structure or for example make required shape by thermoforming.This film can be used for different final uses, for example is used for medical package, drug packages and other industrial uses.Plural layers of the present invention can be used in particular for forming the goods of the 3D shape of thermoforming, for example blister package of medicine or any other barrier packaging.Available method well-known in the art is by forming film and heating and operate around suitable mould.
The moisture vapor transmission rate of this type of film of the present invention (MVTR) can be measured by the described method of ASTM F1249.In preferred embodiments, under 37.8 ℃ and 100% relative humidity, the MVTR of whole plural layers of the present invention is for being less than or equal to the 1.0g/100 inch 2/ day (15.5g/m 2/ day), whole film is preferably the about 0.7g/100 inch of 0.1- 2/ day (the about 10.5g/m of 1.5- 2/ day), whole film is the about 0.06g/100 inch of 0.01-more preferably 2/ day (the about 0.93g/m of 0.15- 2/ day), measure by vapor permeability measuring instrument (for example available from Mocon commodity).
The oxygen permeability of various films of the present invention (OTR) can use OX-TRAN 2/20 instrument (Mocon production), measures by the method for ASTM D-3985 under 23 ℃, 0% relative humidity.In preferred embodiments, the OTR of whole plural layers of the present invention is for being less than or equal to about 50 milliliters/100 inches 2/ day (775g/m 2/ day), be preferably about 20 milliliters/100 inches of about 0.001- 2/ day (the about 310g/m of 0.015- 2/ day), about 10 milliliters/100 inches of more preferably about 0.001- 2/ day (the about 150 milliliters/m of 0.015- 2/ day).
Thin fluoropolymer base film also can be attached to two relative faces of carrier layer, and this also within the scope of the invention.In this embodiment, will repeat above-mentioned identical step, second bottom and the second receiver sheet adhesive lamination are subsequently with described carrier layer delamination.
Following non-restrictive example is in order to explanation the present invention.
Embodiment 1
By the double-deck fluoropolymer/polyolefin film of calendered film method coextrusion.The film of extruding contains enough anti-blocking agents at bottom and/or carrier layer, stops extruding the back with the web-like adhesion.The average thickness of base fluoropolymer layer is about 0.3 mil (7.62 μ m).The average thickness of carrier film is about 2 mils (50 μ m).This fluoro-containing copolymer film is the PCTFE homopolymers.This carrier film is low density polyethylene (LDPE) (LDPE), does not use binding resin to adhere to that this is two-layer.In order to improve the bonding of PCTFE layer and receiver sheet, the one side that bottom exposes is carried out sided corona treatment, the film minimal surface energy that is produced is 45 dyne, surface energy is measured by the surface energy pen or is tested by the water contact angle technology.
Be coated with two component polyurethane adhesive on the exposure of base fluoropolymer layer, this adhesive is made up of 100 parts of epoxy/amine and 12 parts of polyalcohol/isocyanates, and coating speed is 1.5lb/ream (3000 square feet) (2.4g/m 2).Use the Faustal coater/laminator, adopt runner intaglio plate painting method application of adhesive.
Under 160  (71 ℃), adhesive is forced in the aire tunnel formula baking oven dry 20 seconds in routine, direct lamination in conjunction with clamp device at room temperature subsequently, pressure is enough to make the PVC receiver sheet with 1.5 mils (38 μ m) to adhere to.The laminated material that obtains is wound on the axle.
After curing in 24 hours, the bottom with adhesive lamination in separation process separates from carrier layer.Fluoropolymer of lamination (bottom) and PVC (receiver sheet) laminated material are wound on the axle, and polyethylene (carrier) layer is wound on another axle simultaneously.
The MVTR of this film laminate (moisture vapor transmission rate) is the 0.06g/100 inch 2/ day (0.93g/m 2/ day).
Embodiment 2
Repeat embodiment 1, difference has been to prepare the coextrusion carrier film that contains independent resin bed.This carrier film is the individual course of the linear low density polyethylene (LLDPE) (LLDPE) of the tack coat (tie layer) (with polyethylene mixed be made up of ethylene-vinyl acetate) of one deck 0.2 mil (5 μ m) and one deck 1 mil (25 μ m).This tie layer surface contacts with this LLDPE layer with the PCTFE layer resin of 0.3 mil (7.62 μ m).Ply adhesion between tack coat and the fluoro-containing copolymer film enough is weaker than the ply adhesion between tack coat and the LLDPE layer, causes when separating on slitting shears, and fluoro-containing copolymer film is separated from tack coat/LLDPE carrier film.The MVTR of resulting laminated material is the 0.06g/100 inch 2/ day (0.93g/m 2/ day).
Embodiment 3
Repeat embodiment 2, difference is that second face of fluoro-containing copolymer film is coated with the adhesive among the embodiment 1, and is dry in baking oven, directly with the transparent PVC film lamination of 0.7 mil (17.8 μ m).After discovery and the PVC film lamination, this carrier layer of being made up of tack coat and LLDPE breaks away from from the first surface of this fluoro-containing copolymer film at an easy rate.The MVTR of this laminated material is the 0.06g/100 inch 2/ day (0.93g/m 2/ day).
Embodiment 4
Repeat embodiment 2, difference is in extrusion, carried out online machine traffic direction orientation with the draw ratio of 1.5-1.When this fluoropolymer base film was separated from this carrier film, the thickness of this fluoro-containing copolymer film was 0.2 mil (5 μ m), and MVTR is the 0.03g/100 inch 2/ day (0.47g/m 2/ day).
The invention provides fluoro-containing copolymer film extremely thin on receiver sheet as can be seen, method is simple, cost benefit is high.

Claims (40)

1. thin film lamination-delamination process said method comprising the steps of:
A) provide carrier layer with first and second surfaces;
B) base fluoropolymer layer of one deck at least that will have first and second surfaces is applied at least one surface of described carrier layer, the described first surface of the described bottom of one deck at least contacts with the surface of described carrier layer, and the thickness of wherein said bottom is less than or equal to 10.2 μ m;
C) adhesive layer is applied to the described second surface of described bottom;
D) make described bottom be attached to receiver sheet by described adhesive layer; With
E) separate described carrier layer from described bottom, make described bottom still be attached to described receiver sheet.
2. the method for claim 1, described method also are included in carries out step b)-e) on the described second surface of described carrier layer.
3. the process of claim 1 wherein that the thickness of described bottom is less than 10.2 μ m.
4. the process of claim 1 wherein that the thickness of described bottom is 1 μ m-10.2 μ m.
5. the method for claim 1, described method also comprises by intermediate adhesion layer makes described carrier layer be attached to described fluoropolymer layer.
6. the process of claim 1 wherein that plunger bond strength between described bottom and the described carrier layer is less than the bonding strength between described bottom and the described receiver sheet.
7. the process of claim 1 wherein that bonding strength between described bottom and the described receiver sheet is at least 2 times of plunger bond strength between described bottom and the described carrier layer.
8. the process of claim 1 wherein that bonding strength between described bottom and the described receiver sheet is at least 3 times of plunger bond strength between described bottom and the described carrier layer.
9. the process of claim 1 wherein bonding strength between described bottom and the described receiver sheet greater than 79g/cm, the plunger bond strength between described bottom and the described carrier layer is less than 35g/cm.
10. the process of claim 1 wherein that described carrier layer comprises is selected from following material: polyolefin, polyamide, polyester, polyurethane, polyvinyl chloride, ethylene-vinyl acetate, cyclic olefin polymer and blend thereof.
11. the process of claim 1 wherein that described fluoro-containing copolymer film layer comprises is selected from following material: ethylene-chlorotrifluoro-ethylene copolymer, ethylene-tetrafluoroethylene copolymer, fluorinated ethylene-propylene copolymer, perfluoroalkyl ethylene oxy, polytrifluorochloroethylene, polytetrafluoroethylene (PTFE), polyvinyl fluoride, polyvinylidene fluoride and copolymer thereof and blend.
12. the process of claim 1 wherein that described fluoro-containing copolymer film layer comprises polytrifluorochloroethylene.
13. the process of claim 1 wherein that described receiver sheet comprises is selected from following material: polyolefin, polyvinyl chloride, polyester, polyamide, ethylene-propylene acetoacetic ester, ethylene-acrylic acid, cyclic olefin polymer, fabric and paper.
14. the process of claim 1 wherein that described receiver sheet comprises polyvinyl chloride.
15. the process of claim 1 wherein that described support sheet comprises is selected from following polyethylene: ultra-low density polyethylene, low density polyethylene (LDPE), linear low density polyethylene (LLDPE), metallocene linear low density polyethylene (LLDPE), medium density polyethylene, high density polyethylene (HDPE) and combination thereof.
16. the process of claim 1 wherein that described support sheet comprises linear low density polyethylene (LLDPE).
17. the process of claim 1 wherein that described adhesive layer comprises is selected from following material: polyurethane, epoxides, polyester, acrylic compounds, anhydride modified polyolefin, anhydride modified alpha-olefin, polypropylene, the ethylene acid copolymer resin, the copolymer of acrylic or methacrylic acid modification, metallocene polymerising ethylene copolymer, ethylene-vinyl acetate copolymer, sour and anhydride modified polyacrylate and olefin-acrylic ester copolymer, epoxide modified polyolefin, sour and anhydride modified elastomer, s-B-S rubber and blend thereof.
18. the process of claim 1 wherein that described bottom and described carrier layer coextrusion form.
19. the process of claim 1 wherein that described adhesive layer is applied on the described bottom by coating.
20. the process of claim 1 wherein that described receiver sheet is attached to described bottom by described adhesive layer through lamination.
21. the process of claim 1 wherein and with described sheet material described carrier layer is separated from described bottom by tearing described carrier layer.
22. a thin film lamination-delamination process said method comprising the steps of:
A) provide the carrier layer that comprises polyolefin and have first and second surfaces;
B) at least one strata CTFE bottom that will have first and second surfaces is applied at least one surface of described carrier layer, the described first surface of the described bottom of one deck at least contacts with the surface of described carrier layer, and described underlayer thickness is less than or equal to 10.2 μ m;
C) adhesive layer is applied to the described second surface of described bottom;
D) make described bottom be attached to the polyvinyl chloride receiver sheet by described adhesive layer; With
E) separate described carrier layer from described bottom, make described bottom still be attached to described receiver sheet.
23. the method for claim 22, the bonding strength between wherein said bottom and the described receiver sheet are at least 2 times of plunger bond strength between described bottom and the described carrier layer.
24. plural layers, described plural layers comprise:
A) has the carrier layer on first and second surfaces;
B) at least one lip-deep base fluoropolymer layer of one deck at least with first and second surfaces of described carrier layer, the first surface of the described bottom of one deck at least contacts with the surface of described carrier layer; The thickness of wherein said bottom is less than or equal to 10.2 μ m;
C) adhesive layer on the second surface of described bottom; With
D) be attached to the receiver sheet of described bottom, make described adhesive layer contact with described receiver sheet.
25. the plural layers of claim 24, described plural layers also comprise the intermediate adhesion layer between described carrier layer and described fluoropolymer layer.
26. the plural layers of claim 24, the bonding strength between wherein said bottom and the described receiver sheet are at least 2 times of plunger bond strength between described bottom and the described carrier layer.
27. the plural layers of claim 24, the bonding strength between wherein said bottom and the described receiver sheet are greater than 79g/cm, the plunger bond strength between described bottom and the described carrier layer is less than 35g/cm.
28. the plural layers of claim 24, the thickness of wherein said bottom are 1 μ m-10.2 μ m.
29. the plural layers of claim 24, the thickness of wherein said bottom are 2 μ m-10.2 μ m.
30. the plural layers of claim 24, the thickness of wherein said carrier layer are 25 μ m-150 μ m.
31. comprising, the plural layers of claim 24, wherein said carrier layer are selected from following material: polyolefin, polyamide, polyester, polyurethane, polyvinyl chloride, ethylene-vinyl acetate, cyclic olefin polymer and blend thereof.
32. comprising, the plural layers of claim 24, wherein said fluoro-containing copolymer film layer are selected from following material: ethylene-chlorotrifluoro-ethylene copolymer, ethylene-tetrafluoroethylene copolymer, fluorinated ethylene-propylene copolymer, perfluoroalkyl ethylene oxy, polytrifluorochloroethylene, polytetrafluoroethylene (PTFE), polyvinyl fluoride, polyvinylidene fluoride and copolymer thereof and blend.
33. the plural layers of claim 24, wherein said fluoro-containing copolymer film layer comprises polytrifluorochloroethylene.
34. the plural layers of claim 33, the bonding strength between wherein said bottom and the described receiver sheet are at least 2 times of plunger bond strength between described bottom and the described carrier layer.
35. comprising, the plural layers of claim 24, wherein said receiver sheet are selected from following material: polyolefin, polyvinyl chloride, polyester, polyamide, ethylene-propylene acetoacetic ester, ethylene-acrylic acid, cyclic olefin polymer, fabric and paper.
36. comprising, the plural layers of claim 35, wherein said receiver sheet are selected from following polyethylene: ultra-low density polyethylene, low density polyethylene (LDPE), linear low density polyethylene (LLDPE), metallocene linear low density polyethylene (LLDPE), medium density polyethylene, high density polyethylene (HDPE) and combination thereof.
37. the plural layers of claim 24, wherein said receiver sheet comprises polyvinyl chloride.
38. comprising, the plural layers of claim 24, wherein said adhesive layer are selected from following material: polyurethane, epoxides, polyester, acrylic compounds, anhydride modified polyolefin, anhydride modified alpha-olefin, polypropylene, the ethylene acid copolymer resin, the copolymer of acrylic or methacrylic acid modification, metallocene polymerising ethylene copolymer, ethylene-vinyl acetate copolymer, sour and anhydride modified polyacrylate and olefin-acrylic ester copolymer, epoxide modified polyolefin, sour and anhydride modified elastomer, s-B-S rubber and blend thereof.
39. the plural layers of claim 24, wherein said bottom and described carrier layer coextrusion form.
40. the plural layers of claim 24, described plural layers comprise:
A) has the polyolefin carrier layer on first and second surfaces;
B) at least one lip-deep at least one strata CTFE base fluoropolymer layer with first and second surfaces of described carrier layer, the first surface of the described bottom of one deck at least contacts with the surface of described carrier layer; The thickness of wherein said bottom is 1 μ m-10.2 μ m;
C) adhesive layer on the second surface of described bottom; With
D) be attached to the polyvinyl chloride receiver sheet of described bottom, make described adhesive layer contact with described receiver sheet.
CNB2004800081893A 2003-01-27 2004-01-26 Thin film lamination-delamination process for fluoropolymers Expired - Fee Related CN100344447C (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US10/351,920 US6887334B2 (en) 2003-01-27 2003-01-27 Thin film lamination-delamination process for fluoropolymers
US10/351,920 2003-01-27

Publications (2)

Publication Number Publication Date
CN1764538A CN1764538A (en) 2006-04-26
CN100344447C true CN100344447C (en) 2007-10-24

Family

ID=32735879

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB2004800081893A Expired - Fee Related CN100344447C (en) 2003-01-27 2004-01-26 Thin film lamination-delamination process for fluoropolymers

Country Status (7)

Country Link
US (1) US6887334B2 (en)
EP (1) EP1587680A1 (en)
JP (1) JP2006517880A (en)
KR (1) KR20050095878A (en)
CN (1) CN100344447C (en)
TW (1) TW200502094A (en)
WO (1) WO2004069533A1 (en)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7096686B2 (en) * 2004-03-04 2006-08-29 Follett Corporation Ice making apparatus
US7939150B2 (en) * 2005-08-16 2011-05-10 Honeywell International Inc. Lid stock using oriented fluoropolymers
US8980430B2 (en) 2006-08-28 2015-03-17 Frank J. Colombo PCTFE film with extrusion coating of EVA or EVA with UV absorbers
US20090162652A1 (en) * 2007-12-21 2009-06-25 Ranade Aditya P Co-extruded fluoropolymer multilayer laminates
AU2009212751B2 (en) * 2008-02-05 2013-02-07 Saint-Gobain Performance Plastics Corporation Multi-layer article
EP2111982A1 (en) * 2008-04-25 2009-10-28 Amcor Flexibles Transpac N.V. Method for the production of thin polymer film
US8859102B2 (en) * 2008-11-12 2014-10-14 Saint-Gobain Performance Plastics Corporation Barrier structure and method for making
KR20110082612A (en) * 2008-11-12 2011-07-19 생-고뱅 퍼포먼스 플라스틱스 코포레이션 Barrier structure and method for making
US9028123B2 (en) 2010-04-16 2015-05-12 Flex Lighting Ii, Llc Display illumination device with a film-based lightguide having stacked incident surfaces
CN103038568A (en) 2010-04-16 2013-04-10 弗莱克斯照明第二有限责任公司 Front illumination device comprising a film-based lightguide
EP2558775B1 (en) 2010-04-16 2019-11-13 FLEx Lighting II, LLC Illumination device comprising a film-based lightguide
KR101207056B1 (en) * 2010-07-22 2012-11-30 주식회사 엘지화학 Fluoro-based polymer thin layer and method for preparing the same
JP5190553B1 (en) * 2012-03-06 2013-04-24 フリージア・マクロス株式会社 Metal foil with carrier
CN103756100A (en) * 2014-01-22 2014-04-30 苏州新区特氟龙塑料制品厂 Teflon plastic film
KR101601403B1 (en) * 2014-04-01 2016-03-09 현대자동차주식회사 The interfacial strength measuring apparatus and method for a gas diffusion layer of fuel cells
US20170313045A1 (en) * 2014-11-04 2017-11-02 B4H Sa Manufacturing process for glue-less multi-layer decorated film and thermoformed product obtained therewith
JP6578444B2 (en) 2015-08-31 2019-09-18 コンバーター マニュファクチャリング，エルエルシー Formed thermoplastic article having smooth edges
EP3353083A4 (en) * 2015-09-24 2019-05-01 Converter Manufacturing, LLC Moldable container liner having barrier properties
CN108698387B (en) 2016-01-28 2020-05-12 罗杰斯公司 Wire and cable coated with fluoropolymer composite film
JP7187656B2 (en) * 2017-03-17 2022-12-12 藤森工業株式会社 Laminates, blister containers, and press-through packages
JP2018154056A (en) 2017-03-17 2018-10-04 藤森工業株式会社 Laminate, blister container, and press-through package
JP7187657B2 (en) * 2017-03-17 2022-12-12 藤森工業株式会社 Laminates, blister containers, and press-through packages
WO2023235135A1 (en) * 2022-06-03 2023-12-07 Basf Se Co-extruded hdpe and tpu films

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4677017A (en) * 1983-08-01 1987-06-30 Ausimont, U.S.A., Inc. Coextrusion of thermoplastic fluoropolymers with thermoplastic polymers
WO1999024256A1 (en) * 1997-11-06 1999-05-20 Alliedsignal Inc. Multilayered halopolymer poly(alkylene naphthalate) films with uv blocking characteristics
US6296732B1 (en) * 1995-06-07 2001-10-02 Avery Dennison Corporation Extrusion process for protective coatings for outdoor siding panels and the like

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3481910A (en) 1965-10-04 1969-12-02 Eastman Kodak Co Reaction products of unsaturated dicarboxylic acids,anhydrides,esters with degraded poly - alpha - olefin polymers
US3480580A (en) 1965-10-22 1969-11-25 Eastman Kodak Co Modified polymers
US4510301A (en) 1982-06-01 1985-04-09 E. I. Du Pont De Nemours And Company Fluorocarbon copolymer films
JPS6056532A (en) 1983-09-09 1985-04-02 Unitika Ltd Manufacture of fluorine group stretched film
US4544721A (en) 1983-10-06 1985-10-01 E. I. Du Pont De Nemours And Company Chlorotriflouroethylene polymer oriented films
FR2563156B1 (en) 1984-04-19 1987-01-30 Solvay MULTIPLE POLYMERIC LAYER STRUCTURES INCLUDING A VINYL OR VINYLIDENE FLUORIDE POLYMER LAYER LINKED TO A POLAR POLYMER LAYER
JPS61276808A (en) 1985-05-31 1986-12-06 Ube Ind Ltd Maleic acid-modified polyolefin and production thereof
CA1236613A (en) 1985-06-27 1988-05-10 Chun S. Wong Process for the grafting of monomers onto polyolefins
US4826955A (en) 1988-01-21 1989-05-02 Allied-Signal Inc. Amorphous copolyamide article of manufacture with moisture-insensitive oxygen barrier properties
CA2010320C (en) 1989-02-20 2001-04-17 Yohzoh Yamamoto Sheet or film of cyclo-olefin polymer
US5139878A (en) 1991-08-12 1992-08-18 Allied-Signal Inc. Multilayer film constructions
JPH05213000A (en) * 1992-02-03 1993-08-24 Nitto Denko Corp Fluorine film transfer sheet
KR100235089B1 (en) 1992-05-14 1999-12-15 Mitsui Chemicals Inc Ptp or blister packaging articles and packaging material therefor
AU693491B2 (en) 1993-11-19 1998-07-02 Honeywell International, Inc. Polyamide compositions comprising aliphatic polyamide and anaromatic polyamide oligomer having improved moisture resistance
JP3428171B2 (en) * 1994-09-09 2003-07-22 旭硝子株式会社 Coated paper and method for producing the same
US5817386A (en) * 1996-03-28 1998-10-06 Norton Performance Plastics Corporation Silicone-free release films
KR100220961B1 (en) 1996-04-11 1999-09-15 사또 아끼오 Laminated film and packaging material
JP4395211B2 (en) * 1998-01-19 2010-01-06 三菱樹脂株式会社 Fluoropolymer laminated film

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4677017A (en) * 1983-08-01 1987-06-30 Ausimont, U.S.A., Inc. Coextrusion of thermoplastic fluoropolymers with thermoplastic polymers
US6296732B1 (en) * 1995-06-07 2001-10-02 Avery Dennison Corporation Extrusion process for protective coatings for outdoor siding panels and the like
WO1999024256A1 (en) * 1997-11-06 1999-05-20 Alliedsignal Inc. Multilayered halopolymer poly(alkylene naphthalate) films with uv blocking characteristics

Also Published As

Publication number Publication date
TW200502094A (en) 2005-01-16
US20040144482A1 (en) 2004-07-29
WO2004069533A1 (en) 2004-08-19
CN1764538A (en) 2006-04-26
KR20050095878A (en) 2005-10-04
EP1587680A1 (en) 2005-10-26
JP2006517880A (en) 2006-08-03
US6887334B2 (en) 2005-05-03

Similar Documents

Publication Publication Date Title
CN100344447C (en) Thin film lamination-delamination process for fluoropolymers
CA2533694C (en) Multilayer oriented high-modulus film
JP5296378B2 (en) Composition comprising ethylene-acrylate copolymer and polyolefin and tackifier
JP2744132B2 (en) Multilayer film structure
CN101374658B (en) Multilayer oriented film
EP1749655B1 (en) Multilayer Coextruded Films Including Frangible Intralaminar Bonding Forces
EP1574328B1 (en) Packaging films containing coextruded polyester and nylon layers
EP0504808B1 (en) Multi-layer construction film and method for producing same
CN1662372A (en) Blister package
US20110039098A1 (en) Gas-barrier films and sheets
US20060251876A1 (en) Sealable, multilayer, coextruded packaging film, its use and process for its production
CN1151713A (en) Film compsn.
CN101594991B (en) There is the PCTFE film of EVA or the extruding coating containing the EVA of UV absorbent
PL207071B1 (en) Multilayer packaging structures
KR100766349B1 (en) Stretched polyamide film
CN1894095A (en) Lamination adhesion of foil to thermoplastic polymers
US20210354894A1 (en) Recyclable Packaging Laminate Having A Good Barrier Effect And Low Density, And Method For The Production Thereof
CN1227524A (en) Multilayer polyamide film structures
FI73923C (en) Polyamide-containing multilayer film
US8986823B1 (en) Microlayer extrusion coating and laminating for flexible packaging
JPH08267676A (en) Coextrusion composite film for laminate
CN1760087A (en) Composite packaging film including five layers being extruded out capable of obstructing liquid highly
AU2004261401B2 (en) Multilayer oriented high-modulus film
JPH1052892A (en) Gas barrier multilayer film
KR20200084635A (en) Barrier film

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20071024

Termination date: 20100228